HGVS | Genome Assembly |
---|---|
NC_000023.11:g.132128009C>A , CM000685.2:g.132128009C>A | GRCh38 |
NC_000023.10:g.131262037C>A , CM000685.1:g.131262037C>A | GRCh37 |
NC_000023.9:g.131089718C>A | NCBI36 |
NG_012347.1:g.5014G>T , LRG_867:g.5014G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000298542.9:c.-165G>T MANE Select | ENSP00000298542.3:n.-165G>T | |
ENST00000298542.8:c.-165G>T | ENSP00000298542.3:n.-165G>T | |
NM_001306193.1:c.-165G>T | NP_001293122.1:n.-165G>T | |
NM_194277.2:c.-165G>T , LRG_867t1:c.-165G>T | NP_919253.1:n.-165G>T | |
NM_001306193.2:c.-165G>T | NP_001293122.1:n.-165G>T | |
NM_194277.3:c.-165G>T MANE Select | NP_919253.1:n.-165G>T |